24 results · 28ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

MICRODOSE CATH, MODELS 90121-201, -202, -203

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

Zirlux

FDA UDI
HENRY SCHEIN, INC.·H65890113831·Zirlux Scan Abut Blue 3.0

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033273951·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033357866·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033273937·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033273920·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033273944·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033273968·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033273906·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033357910·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033273913·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033273975·

MR Detergent Solution

FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06936415904678·

TEMP SCAN

FDA 510(k)
FDA Class 2 ·General Hospital

SUPREMCAST V

FDA 510(k)
FDA Class 2 ·Dental

UNKNOWN

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 15, 2025

LEVEL 1 HOTLINE LOW FLOW SYSTEMS

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

LEVEL 1 HOTLINE LOW FLOW SYSTEMS

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LGZ·January 23, 2024

GOBED II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 19, 2013

UNKNOWN DEPUY ASR HIP

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·March 4, 2011